Yu Peng, Xueqin Guo, Yawei Fan, Han Liu, Leiqian Sun, Di Liu, Hui Li, Xin Wang, Hongli Guo, Hai Lu
{"title":"Identifying a <i>cis-element</i> in PtoCP1 promoter for efficiently controlling constitutive gene expression in <i>Populus tomentosa</i>.","authors":"Yu Peng, Xueqin Guo, Yawei Fan, Han Liu, Leiqian Sun, Di Liu, Hui Li, Xin Wang, Hongli Guo, Hai Lu","doi":"10.7717/peerj.18292","DOIUrl":null,"url":null,"abstract":"<p><p>Gene expression is regulated by transcription factors binding to <i>cis-elements</i> in promoters. However, efficient <i>cis-elements</i> for genetic engineering are rarely reported. In this study, we identified an 11 bp <i>cis-element</i> in the PtoCP1 promoter that drives strong constitutive gene expression in <i>Populus tomentosa</i>. A 2,270 bp promoter region upstream of the <i>PtoCP1</i> gene's translation start site was cloned and named ProPtoCP1. This promoter controls GUS reporter gene expression in the roots, leaves, and stems of <i>Arabidopsis</i> seedlings. Based on the location and density of <i>cis-elements</i>, the PtoCP1 promoter was divided into four fragments by 5'-end deletions. GUS staining and RT-qPCR revealed a key <i>cis-element</i> at -466 to -441 bp essential for gene expression. Further analysis showed that the MYB-TGACG <i>cis-element</i> is a positive regulator, whereas neither MYB nor TGACG alone drove gene expression. This study enhances our understanding of gene expression regulation by <i>cis-elements</i> and provides a valuable tool for genetic engineering.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11505885/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7717/peerj.18292","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Gene expression is regulated by transcription factors binding to cis-elements in promoters. However, efficient cis-elements for genetic engineering are rarely reported. In this study, we identified an 11 bp cis-element in the PtoCP1 promoter that drives strong constitutive gene expression in Populus tomentosa. A 2,270 bp promoter region upstream of the PtoCP1 gene's translation start site was cloned and named ProPtoCP1. This promoter controls GUS reporter gene expression in the roots, leaves, and stems of Arabidopsis seedlings. Based on the location and density of cis-elements, the PtoCP1 promoter was divided into four fragments by 5'-end deletions. GUS staining and RT-qPCR revealed a key cis-element at -466 to -441 bp essential for gene expression. Further analysis showed that the MYB-TGACG cis-element is a positive regulator, whereas neither MYB nor TGACG alone drove gene expression. This study enhances our understanding of gene expression regulation by cis-elements and provides a valuable tool for genetic engineering.